Incidental Mutation 'R6180:Mug2'
| ID |
487990 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Mug2
|
| Ensembl Gene |
ENSMUSG00000030131 |
| Gene Name |
murinoglobulin 2 |
| Synonyms |
|
| MMRRC Submission |
044322-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.054)
|
| Stock # |
R6180 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
6 |
| Chromosomal Location |
122006761-122085965 bp(+) (GRCm38) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 122079606 bp (GRCm38)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glutamic Acid to Glycine
at position 1170
(E1170G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000080469
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000081777]
|
| AlphaFold |
P28666 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000081777
AA Change: E1170G
PolyPhen 2
Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
|
| SMART Domains |
Protein: ENSMUSP00000080469
Gene: ENSMUSG00000030131
AA Change: E1170G
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:A2M_N
|
128 |
221 |
3.5e-21 |
PFAM |
|
A2M_N_2
|
449 |
599 |
1.05e-42 |
SMART |
|
low complexity region
|
711 |
728 |
N/A |
INTRINSIC |
|
A2M
|
740 |
830 |
7.16e-36 |
SMART |
|
Pfam:Thiol-ester_cl
|
963 |
992 |
1e-18 |
PFAM |
|
low complexity region
|
994 |
1005 |
N/A |
INTRINSIC |
|
Pfam:A2M_comp
|
1012 |
1097 |
5.8e-34 |
PFAM |
|
Pfam:A2M_comp
|
1093 |
1243 |
3e-47 |
PFAM |
|
A2M_recep
|
1353 |
1440 |
1.85e-38 |
SMART |
|
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.6%
- 10x: 98.1%
- 20x: 94.5%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 88 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2610507B11Rik |
A |
G |
11: 78,273,258 (GRCm38) |
M1142V |
possibly damaging |
Het |
| Adam39 |
A |
G |
8: 40,826,573 (GRCm38) |
N667S |
probably benign |
Het |
| Ap4e1 |
T |
A |
2: 127,066,588 (GRCm38) |
C1085* |
probably null |
Het |
| BC035044 |
A |
T |
6: 128,885,034 (GRCm38) |
|
probably benign |
Het |
| Capn11 |
T |
C |
17: 45,630,766 (GRCm38) |
D693G |
probably damaging |
Het |
| Cavin4 |
A |
T |
4: 48,663,917 (GRCm38) |
H99L |
possibly damaging |
Het |
| Ccdc86 |
T |
C |
19: 10,948,581 (GRCm38) |
K218R |
possibly damaging |
Het |
| Ccno |
T |
C |
13: 112,989,845 (GRCm38) |
S283P |
probably damaging |
Het |
| Ccser2 |
A |
T |
14: 36,940,319 (GRCm38) |
S303T |
probably benign |
Het |
| Cd53 |
T |
A |
3: 106,767,364 (GRCm38) |
N129I |
probably damaging |
Het |
| Cd63 |
G |
A |
10: 128,912,064 (GRCm38) |
|
probably null |
Het |
| Cyp2j6 |
G |
C |
4: 96,536,086 (GRCm38) |
L145V |
probably damaging |
Het |
| Daam2 |
A |
G |
17: 49,469,666 (GRCm38) |
M797T |
probably damaging |
Het |
| Dmgdh |
G |
A |
13: 93,752,286 (GRCm38) |
V811I |
possibly damaging |
Het |
| Dpysl4 |
A |
T |
7: 139,090,334 (GRCm38) |
T123S |
probably damaging |
Het |
| Erap1 |
A |
G |
13: 74,666,226 (GRCm38) |
E428G |
possibly damaging |
Het |
| Fam124b |
T |
A |
1: 80,200,185 (GRCm38) |
T366S |
possibly damaging |
Het |
| Fbxw22 |
T |
C |
9: 109,386,679 (GRCm38) |
D167G |
probably damaging |
Het |
| Flrt2 |
C |
T |
12: 95,779,238 (GRCm38) |
Q117* |
probably null |
Het |
| Ftsj3 |
A |
T |
11: 106,253,340 (GRCm38) |
|
probably null |
Het |
| Ggn |
A |
G |
7: 29,173,049 (GRCm38) |
Y618C |
probably damaging |
Het |
| Glis1 |
T |
A |
4: 107,627,513 (GRCm38) |
S402T |
probably benign |
Het |
| Gm13762 |
T |
G |
2: 88,973,882 (GRCm38) |
N3T |
probably damaging |
Het |
| Gm4781 |
T |
A |
10: 100,396,487 (GRCm38) |
|
noncoding transcript |
Het |
| Gm7168 |
T |
A |
17: 13,948,596 (GRCm38) |
I75K |
probably damaging |
Het |
| Gm7298 |
C |
T |
6: 121,760,823 (GRCm38) |
H348Y |
probably benign |
Het |
| Gria1 |
G |
T |
11: 57,242,792 (GRCm38) |
R499L |
probably damaging |
Het |
| Gtf2ird2 |
C |
T |
5: 134,216,547 (GRCm38) |
T549M |
probably damaging |
Het |
| H2-M10.6 |
T |
A |
17: 36,814,286 (GRCm38) |
V323E |
probably damaging |
Het |
| Hoxb3 |
G |
A |
11: 96,346,103 (GRCm38) |
V336I |
probably benign |
Het |
| Il12b |
G |
A |
11: 44,412,626 (GRCm38) |
A327T |
probably benign |
Het |
| Inpp4a |
C |
A |
1: 37,380,102 (GRCm38) |
P588T |
probably benign |
Het |
| Kctd12 |
C |
A |
14: 102,981,591 (GRCm38) |
D284Y |
probably damaging |
Het |
| Kif28 |
C |
A |
1: 179,697,772 (GRCm38) |
|
probably null |
Het |
| Krt2 |
T |
C |
15: 101,815,044 (GRCm38) |
N332S |
probably benign |
Het |
| Lama2 |
G |
A |
10: 26,981,499 (GRCm38) |
T3118I |
probably benign |
Het |
| Lgi1 |
T |
C |
19: 38,264,956 (GRCm38) |
L25P |
probably damaging |
Het |
| Lhx3 |
T |
A |
2: 26,201,491 (GRCm38) |
M269L |
probably benign |
Het |
| Lmtk2 |
A |
T |
5: 144,175,342 (GRCm38) |
E960V |
probably damaging |
Het |
| Loxl4 |
A |
T |
19: 42,608,352 (GRCm38) |
D60E |
probably damaging |
Het |
| Lrp2 |
T |
A |
2: 69,503,524 (GRCm38) |
N1458Y |
possibly damaging |
Het |
| Ltn1 |
A |
T |
16: 87,427,789 (GRCm38) |
S16T |
probably damaging |
Het |
| Mllt6 |
G |
A |
11: 97,678,536 (GRCm38) |
A875T |
possibly damaging |
Het |
| Mpp5 |
C |
T |
12: 78,817,310 (GRCm38) |
H216Y |
probably benign |
Het |
| Mrgprb4 |
A |
T |
7: 48,198,826 (GRCm38) |
I118N |
probably damaging |
Het |
| Mrps7 |
A |
G |
11: 115,604,881 (GRCm38) |
T82A |
possibly damaging |
Het |
| Nav2 |
A |
G |
7: 49,458,167 (GRCm38) |
H647R |
probably benign |
Het |
| Nbeal2 |
T |
C |
9: 110,625,147 (GRCm38) |
Y2710C |
probably damaging |
Het |
| Ndc1 |
A |
T |
4: 107,411,198 (GRCm38) |
I644L |
possibly damaging |
Het |
| Olfr952 |
A |
T |
9: 39,426,712 (GRCm38) |
Y120N |
probably damaging |
Het |
| Padi4 |
A |
G |
4: 140,756,473 (GRCm38) |
M352T |
possibly damaging |
Het |
| Pcdhgc3 |
C |
A |
18: 37,806,937 (GRCm38) |
D130E |
probably damaging |
Het |
| Pde6a |
A |
T |
18: 61,284,092 (GRCm38) |
|
probably null |
Het |
| Pdpn |
C |
T |
4: 143,299,222 (GRCm38) |
G12R |
probably damaging |
Het |
| Pot1a |
A |
T |
6: 25,771,621 (GRCm38) |
D200E |
probably benign |
Het |
| Ppa1 |
A |
T |
10: 61,667,652 (GRCm38) |
D236V |
probably benign |
Het |
| Ptprn2 |
T |
A |
12: 116,859,119 (GRCm38) |
S273T |
probably benign |
Het |
| Rasgrf2 |
T |
C |
13: 92,029,101 (GRCm38) |
E297G |
probably damaging |
Het |
| Rgl1 |
T |
C |
1: 152,519,172 (GRCm38) |
N750S |
probably damaging |
Het |
| Rinl |
A |
G |
7: 28,796,940 (GRCm38) |
N449D |
probably benign |
Het |
| Samd8 |
T |
A |
14: 21,775,025 (GRCm38) |
H79Q |
probably benign |
Het |
| Scn11a |
T |
C |
9: 119,754,867 (GRCm38) |
I1561V |
probably benign |
Het |
| Slc39a12 |
T |
C |
2: 14,396,127 (GRCm38) |
L105P |
probably benign |
Het |
| Slc7a12 |
A |
T |
3: 14,481,140 (GRCm38) |
|
probably null |
Het |
| Slco1a4 |
A |
G |
6: 141,817,820 (GRCm38) |
I390T |
possibly damaging |
Het |
| Snta1 |
T |
C |
2: 154,377,182 (GRCm38) |
N411S |
probably benign |
Het |
| Srgap2 |
T |
C |
1: 131,349,541 (GRCm38) |
T323A |
probably benign |
Het |
| Ssh2 |
G |
T |
11: 77,453,465 (GRCm38) |
V759L |
probably benign |
Het |
| St5 |
A |
C |
7: 109,556,888 (GRCm38) |
D218E |
probably benign |
Het |
| Swap70 |
G |
T |
7: 110,269,981 (GRCm38) |
R327L |
probably damaging |
Het |
| Tbc1d4 |
C |
A |
14: 101,458,770 (GRCm38) |
C914F |
probably benign |
Het |
| Tbx3 |
A |
G |
5: 119,674,067 (GRCm38) |
D144G |
probably damaging |
Het |
| Tgfbr2 |
T |
C |
9: 116,110,144 (GRCm38) |
K205R |
possibly damaging |
Het |
| Tmem94 |
A |
T |
11: 115,791,031 (GRCm38) |
|
probably null |
Het |
| Usf3 |
T |
A |
16: 44,221,105 (GRCm38) |
F1983I |
probably damaging |
Het |
| Ush2a |
T |
A |
1: 188,399,871 (GRCm38) |
C763* |
probably null |
Het |
| Vmn1r115 |
A |
C |
7: 20,844,715 (GRCm38) |
L91V |
probably damaging |
Het |
| Vmn1r201 |
A |
T |
13: 22,475,329 (GRCm38) |
I238F |
possibly damaging |
Het |
| Vmn1r28 |
T |
A |
6: 58,265,491 (GRCm38) |
S106R |
probably damaging |
Het |
| Vmn1r82 |
T |
C |
7: 12,305,085 (GRCm38) |
V95A |
probably damaging |
Het |
| Vrk3 |
A |
T |
7: 44,769,611 (GRCm38) |
N371I |
possibly damaging |
Het |
| Wnt8b |
C |
A |
19: 44,511,643 (GRCm38) |
A223E |
probably benign |
Het |
| Xirp2 |
T |
C |
2: 67,505,577 (GRCm38) |
|
probably null |
Het |
| Xpo7 |
T |
C |
14: 70,682,803 (GRCm38) |
N642S |
probably benign |
Het |
| Ythdc1 |
G |
A |
5: 86,828,094 (GRCm38) |
R520H |
possibly damaging |
Het |
| Zfp367 |
T |
C |
13: 64,135,390 (GRCm38) |
E316G |
probably damaging |
Het |
| Zfp488 |
T |
A |
14: 33,970,794 (GRCm38) |
R137S |
possibly damaging |
Het |
| Zfp532 |
G |
T |
18: 65,656,471 (GRCm38) |
V994L |
probably benign |
Het |
|
| Other mutations in Mug2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00708:Mug2
|
APN |
6 |
122,047,487 (GRCm38) |
missense |
possibly damaging |
0.83 |
|
IGL00957:Mug2
|
APN |
6 |
122,040,654 (GRCm38) |
missense |
probably damaging |
0.99 |
|
IGL01314:Mug2
|
APN |
6 |
122,081,279 (GRCm38) |
missense |
possibly damaging |
0.62 |
|
IGL01338:Mug2
|
APN |
6 |
122,049,628 (GRCm38) |
splice site |
probably benign |
|
|
IGL01477:Mug2
|
APN |
6 |
122,081,684 (GRCm38) |
splice site |
probably benign |
|
|
IGL01926:Mug2
|
APN |
6 |
122,036,104 (GRCm38) |
splice site |
probably benign |
|
|
IGL02019:Mug2
|
APN |
6 |
122,047,435 (GRCm38) |
missense |
probably benign |
0.02 |
|
IGL02305:Mug2
|
APN |
6 |
122,036,056 (GRCm38) |
missense |
probably benign |
|
|
IGL02310:Mug2
|
APN |
6 |
122,059,123 (GRCm38) |
splice site |
probably benign |
|
|
IGL02484:Mug2
|
APN |
6 |
122,072,753 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02516:Mug2
|
APN |
6 |
122,070,843 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02531:Mug2
|
APN |
6 |
122,072,771 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02666:Mug2
|
APN |
6 |
122,081,326 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02936:Mug2
|
APN |
6 |
122,081,387 (GRCm38) |
critical splice donor site |
probably null |
|
|
R0114:Mug2
|
UTSW |
6 |
122,040,648 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0119:Mug2
|
UTSW |
6 |
122,036,063 (GRCm38) |
missense |
probably benign |
0.00 |
|
R0123:Mug2
|
UTSW |
6 |
122,074,714 (GRCm38) |
missense |
possibly damaging |
0.89 |
|
R0144:Mug2
|
UTSW |
6 |
122,071,011 (GRCm38) |
splice site |
probably benign |
|
|
R0225:Mug2
|
UTSW |
6 |
122,074,714 (GRCm38) |
missense |
possibly damaging |
0.89 |
|
R0514:Mug2
|
UTSW |
6 |
122,081,599 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0763:Mug2
|
UTSW |
6 |
122,075,294 (GRCm38) |
missense |
probably benign |
|
|
R0959:Mug2
|
UTSW |
6 |
122,085,495 (GRCm38) |
missense |
probably benign |
0.33 |
|
R1104:Mug2
|
UTSW |
6 |
122,059,055 (GRCm38) |
missense |
probably benign |
|
|
R1239:Mug2
|
UTSW |
6 |
122,081,678 (GRCm38) |
splice site |
probably benign |
|
|
R1318:Mug2
|
UTSW |
6 |
122,077,402 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1460:Mug2
|
UTSW |
6 |
122,040,533 (GRCm38) |
splice site |
probably benign |
|
|
R1706:Mug2
|
UTSW |
6 |
122,036,232 (GRCm38) |
splice site |
probably benign |
|
|
R1761:Mug2
|
UTSW |
6 |
122,074,705 (GRCm38) |
missense |
probably benign |
0.20 |
|
R1901:Mug2
|
UTSW |
6 |
122,071,842 (GRCm38) |
missense |
probably benign |
0.02 |
|
R1913:Mug2
|
UTSW |
6 |
122,070,870 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1943:Mug2
|
UTSW |
6 |
122,079,639 (GRCm38) |
missense |
probably benign |
|
|
R2054:Mug2
|
UTSW |
6 |
122,077,492 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2060:Mug2
|
UTSW |
6 |
122,079,612 (GRCm38) |
missense |
probably benign |
|
|
R2420:Mug2
|
UTSW |
6 |
122,083,460 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2432:Mug2
|
UTSW |
6 |
122,084,376 (GRCm38) |
missense |
possibly damaging |
0.93 |
|
R2916:Mug2
|
UTSW |
6 |
122,074,724 (GRCm38) |
splice site |
probably null |
|
|
R2918:Mug2
|
UTSW |
6 |
122,074,724 (GRCm38) |
splice site |
probably null |
|
|
R3423:Mug2
|
UTSW |
6 |
122,047,506 (GRCm38) |
splice site |
probably benign |
|
|
R3834:Mug2
|
UTSW |
6 |
122,049,787 (GRCm38) |
critical splice donor site |
probably null |
|
|
R3902:Mug2
|
UTSW |
6 |
122,075,567 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R3941:Mug2
|
UTSW |
6 |
122,063,563 (GRCm38) |
missense |
probably benign |
|
|
R4227:Mug2
|
UTSW |
6 |
122,040,732 (GRCm38) |
missense |
probably benign |
0.10 |
|
R4284:Mug2
|
UTSW |
6 |
122,063,673 (GRCm38) |
missense |
probably benign |
0.00 |
|
R4287:Mug2
|
UTSW |
6 |
122,063,673 (GRCm38) |
missense |
probably benign |
0.00 |
|
R4377:Mug2
|
UTSW |
6 |
122,071,007 (GRCm38) |
critical splice donor site |
probably null |
|
|
R4419:Mug2
|
UTSW |
6 |
122,079,630 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4498:Mug2
|
UTSW |
6 |
122,082,752 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R4566:Mug2
|
UTSW |
6 |
122,079,638 (GRCm38) |
missense |
probably benign |
0.00 |
|
R4690:Mug2
|
UTSW |
6 |
122,036,296 (GRCm38) |
missense |
probably benign |
|
|
R4732:Mug2
|
UTSW |
6 |
122,071,872 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R4733:Mug2
|
UTSW |
6 |
122,071,872 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R4741:Mug2
|
UTSW |
6 |
122,079,613 (GRCm38) |
missense |
probably benign |
|
|
R4888:Mug2
|
UTSW |
6 |
122,081,195 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5199:Mug2
|
UTSW |
6 |
122,040,660 (GRCm38) |
missense |
probably benign |
|
|
R5347:Mug2
|
UTSW |
6 |
122,081,592 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5457:Mug2
|
UTSW |
6 |
122,049,729 (GRCm38) |
nonsense |
probably null |
|
|
R5495:Mug2
|
UTSW |
6 |
122,079,650 (GRCm38) |
missense |
probably damaging |
0.96 |
|
R5509:Mug2
|
UTSW |
6 |
122,084,381 (GRCm38) |
missense |
possibly damaging |
0.84 |
|
R6006:Mug2
|
UTSW |
6 |
122,083,500 (GRCm38) |
missense |
probably null |
0.98 |
|
R6184:Mug2
|
UTSW |
6 |
122,037,046 (GRCm38) |
missense |
probably benign |
|
|
R6199:Mug2
|
UTSW |
6 |
122,047,439 (GRCm38) |
missense |
probably benign |
0.05 |
|
R6262:Mug2
|
UTSW |
6 |
122,075,255 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6416:Mug2
|
UTSW |
6 |
122,082,754 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6548:Mug2
|
UTSW |
6 |
122,047,442 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6703:Mug2
|
UTSW |
6 |
122,078,694 (GRCm38) |
missense |
probably benign |
0.25 |
|
R7106:Mug2
|
UTSW |
6 |
122,082,721 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7131:Mug2
|
UTSW |
6 |
122,075,247 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7372:Mug2
|
UTSW |
6 |
122,083,466 (GRCm38) |
missense |
possibly damaging |
0.88 |
|
R7379:Mug2
|
UTSW |
6 |
122,047,487 (GRCm38) |
missense |
possibly damaging |
0.83 |
|
R7419:Mug2
|
UTSW |
6 |
122,040,570 (GRCm38) |
missense |
possibly damaging |
0.86 |
|
R7423:Mug2
|
UTSW |
6 |
122,079,726 (GRCm38) |
missense |
probably benign |
0.00 |
|
R7581:Mug2
|
UTSW |
6 |
122,063,711 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7582:Mug2
|
UTSW |
6 |
122,079,644 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R7672:Mug2
|
UTSW |
6 |
122,040,719 (GRCm38) |
missense |
probably benign |
0.37 |
|
R7713:Mug2
|
UTSW |
6 |
122,078,795 (GRCm38) |
missense |
possibly damaging |
0.83 |
|
R7759:Mug2
|
UTSW |
6 |
122,081,358 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7834:Mug2
|
UTSW |
6 |
122,036,282 (GRCm38) |
missense |
probably benign |
|
|
R7850:Mug2
|
UTSW |
6 |
122,075,211 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8029:Mug2
|
UTSW |
6 |
122,081,545 (GRCm38) |
critical splice acceptor site |
probably null |
|
|
R8127:Mug2
|
UTSW |
6 |
122,075,608 (GRCm38) |
missense |
probably benign |
0.01 |
|
R8335:Mug2
|
UTSW |
6 |
122,040,584 (GRCm38) |
missense |
probably benign |
|
|
R8348:Mug2
|
UTSW |
6 |
122,072,233 (GRCm38) |
nonsense |
probably null |
|
|
R8557:Mug2
|
UTSW |
6 |
122,063,701 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R8798:Mug2
|
UTSW |
6 |
122,081,610 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8823:Mug2
|
UTSW |
6 |
122,063,689 (GRCm38) |
missense |
possibly damaging |
0.89 |
|
R9029:Mug2
|
UTSW |
6 |
122,084,369 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9153:Mug2
|
UTSW |
6 |
122,040,668 (GRCm38) |
missense |
possibly damaging |
0.71 |
|
R9185:Mug2
|
UTSW |
6 |
122,077,483 (GRCm38) |
missense |
probably benign |
0.06 |
|
R9186:Mug2
|
UTSW |
6 |
122,075,289 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R9418:Mug2
|
UTSW |
6 |
122,040,741 (GRCm38) |
missense |
probably benign |
0.00 |
|
R9464:Mug2
|
UTSW |
6 |
122,051,731 (GRCm38) |
missense |
probably benign |
0.01 |
|
R9622:Mug2
|
UTSW |
6 |
122,051,792 (GRCm38) |
missense |
probably benign |
0.29 |
|
Z1177:Mug2
|
UTSW |
6 |
122,037,121 (GRCm38) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- CAATCGATTGCACTCACTGG -3'
(R):5'- AAAACCACCAACCTGTGTGG -3'
Sequencing Primer
(F):5'- GCACTCACTGGAAATTTTTACTGAG -3'
(R):5'- CACCAACCTGTGTGGAGGAG -3'
|
| Posted On |
2017-10-10 |
Incidental Mutation